Summaries of Must-Read Clinical Literature, Guidelines, and FDA Actions
Impact of Earlier Disease-Modifying Therapy
Leuk Res; 2017 Sep; Cogle, Reddy, Chang, et al
Patients with myelodysplastic syndrome who received early disease-modifying therapy (DMT) with azacitidine, decitabine, or lenalidomide were more apt to achieve transfusion independence than those who were given the same type of treatment later, according to a retrospective study involving 508 individuals.
Participants were identified from the SEER registry and Medicare claims from 2006-2012. Investigators estimated the impact of DMT-initiation (≤3 vs >3 months from start of transfusion dependence) on the likelihood of achieving transfusion independence. Among the results:
- Early initiators received DMT within an average of 28 days, vs 187 days for late initiators.
- 62% of early initiators used erythropoiesis-stimulating agents before achieving transfusion independence, vs nearly three-fourths of late initiators.
- Early initiators were 69% more likely to achieve transfusion independence.
- Patients who met minimum active therapy-exposure requirements were more than twice as likely to achieve such.
Cogle C, Reddy S, Chang E, et al. Early treatment initiation in lower-risk myelodysplastic syndromes produces an earlier and higher rate of transfusion independence. Leuk Res. 2017;60:123-128. doi:10.1016/j.leukres.2017.07.008.
This Week's Must Reads
Must Reads in AML
Immune system changes play a role in AML relapse, Christopher MJ et al. N Engl J Med. 2018 Oct 31. doi: 10.1056/NEJMoa1808777.
Venetoclax plus HMA studied in AML, DiNardo C et al. Blood. 2018 Oct 25. doi: 10.1182/blood-2018-08-868752.
T cell infusion effective in PML, Muftuoglu M et al. N Engl J Med. 2018 Oct 11;379:1443-51
Higher AML, MDS risk linked to autotransplants, Radivoyevitch T et al. Leuk Res. 2018 Jul 19. pii: S0145-2126(18)30160-7
Tibsovo for AML with IDH1 mutation, FDA approves first targeted treatment for patients with relapsed or refractory acute myeloid leukemia who have a certain genetic mutation, FDA press release
